Variant report

Variant rs17131677
Chromosome Location chr1:93464587-93464588
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:93451800-93466000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr1:93459800-93466000 Weak transcription Brain Anterior Caudate brain
3 chr1:93459800-93466000 Weak transcription GM12878-XiMat blood
4 chr1:93461800-93466000 Weak transcription Pancreas Pancrea
5 chr1:93462200-93465200 Weak transcription Fetal Intestine Small intestine
6 chr1:93462200-93465800 Weak transcription Stomach Mucosa stomach
7 chr1:93462800-93466000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr1:93463200-93465800 Weak transcription Brain Cingulate Gyrus brain
9 chr1:93463800-93464600 Enhancers Fetal Intestine Large intestine
10 chr1:93463800-93465600 Weak transcription iPS-15b Cell Line embryonic stem cell
11 chr1:93463800-93466000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr1:93463800-93466000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr1:93463800-93466000 Weak transcription Placenta Placenta
14 chr1:93463800-93467600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
15 chr1:93464400-93464800 Enhancers Fetal Muscle Leg muscle

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